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Fully Remove

EUDAMED

Class IIa (EU MDR)

Ref VKFU-1517-AMS

by Biopsybell Srl

Identity

Trade Name
FULLY REMOVE EUDAMED
VERT-BIOPSY EUDAMED
Device Name
FULLY REMOVE EUDAMED
NEEDLES FOR BIOPSY OR EXPLANT EUDAMED
Model / Reference
VKFU-1517-AMS EUDAMED

Identifiers

Primary DI / UDI-DI
08033860027797 EUDAMED
Basic UDI-DI
B-08033860027797 EUDAMED
8033860BIOEFT01U5 EUDAMED
EMDN Code
A01020201 ILIAC-STERNAL BIOPSY NEEDLES AND KITS EUDAMED
A01020203 VERTEBRAL AND PARAVERTEBRAL BIOPSY NEEDLES AND KITS EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Italy EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Fully Remove by Biopsybell Srl — Class IIa — MDR, MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

European Union Active

CE/MDD

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Manufacturer

Manufacturer
Biopsybell Srl
EUDAMED SRN
IT-MF-000011601

Sources (2)

  • EUDAMED 7a313770-7460-4f67-9080-b2c708df4294 61 fields · synced Jun 18, 2026
  • EUDAMED 6bce5023-d614-4490-9c33-598370a6adf4 61 fields · synced May 19, 2026